Synthesis of Zintl Phase Metal Silicide Thermoelectric Materials in Magnesium/Zinc Flux

Zintl phases have potential applications as thermoelectric materials for power generation and cooling owing to their complex crystal structures and unique electronic properties. We carried out reactions of silicon with barium and strontium in excess Mg/Zn flux to synthesize (Ba/Sr)5+xMg19‑xSi12 Zint...

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Published inInorganic chemistry Vol. 63; no. 43; pp. 20186 - 20196
Main Authors Zareihassangheshlaghi, Amirhossein, Galeano-Cabral, Jorge, Uddin, Md Sahab, Schundelmier, Benny, Wei, Kaya, Baumbach, Ryan E., Latturner, Susan E.
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 28.10.2024
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Summary:Zintl phases have potential applications as thermoelectric materials for power generation and cooling owing to their complex crystal structures and unique electronic properties. We carried out reactions of silicon with barium and strontium in excess Mg/Zn flux to synthesize (Ba/Sr)5+xMg19‑xSi12 Zintl phases, investigating the effect of varying Ba/Sr ratio on site mixing and thermoelectric properties. (Ba/Sr)5+xMg19‑xSi12 compounds with 0 < x < 3 are charge-balanced Zintl phases which adopt the hexagonal Ho5Ni19P12 structure type (space group P6̅2m). Density of states calculations indicate that these materials are semimetals. Single-crystal X-ray diffraction data and elemental analysis for Ba5Mg19Si12, Ba4.86Sr2.94Mg16.20Si12, Ba3.63Sr4.20Mg16.17Si12, Ba1.93Sr5.99Mg16.08Si12, and Sr7.82Mg16.18Si12 show occupation of barium and strontium cations in Ho sites, while strontium mixes with magnesium on a specific Ni site. Powder XRD data of products show that they are single phase throughout the sample. Thermoelectric measurements indicate that increasing strontium content and mixing on three cation sites decreases thermal conductivity; it is hypothesized that improved overall thermoelectric behavior is likely due to the rattling of the Sr cations in their positions.
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ISSN:0020-1669
1520-510X
1520-510X
DOI:10.1021/acs.inorgchem.4c01079